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FDA approval of life-saving SMA drug is hailed by its researcher-inventor at CSHL

‘A perfect example of why we do basic research,’ says Dr. Bruce Stillman, CSHL president

Cold Spring Harbor, NY — Within a week of Christmas day, a drug called nusinersen (Spinraza) will be in the hands of doctors across the nation, who will use it, most urgently, to treat young children with a severe and potentially fatal illness called spinal muscular atrophy (SMA).

The leading genetic cause of infant mortality, SMA is a motor neuron disease that leads to the wasting of young muscles, impairing the ability of newborns and toddlers to walk, crawl, or even hold their heads up, and in the most severe cases, failure of muscles that enable them to breathe.

Dr Adrian Krainer and Emma LarsonNusinersen's inventor, research scientist Dr. Adrian Krainer of CSHL, with Emma Larson, a 3 year old who has been helped by the newly approved drug. (click to enlarge)Nusinersen (to be sold by Biogen under the brand name Spinraza) was conceived and tested over several years in mouse models of SMA by Professor Adrian Krainer, Ph.D., and his colleagues at Cold Spring Harbor Laboratory (CSHL) in collaboration with drug developers led by Dr. Frank Bennett at Ionis Pharmaceuticals. Their collaboration began a dozen years ago.

“Some are understandably calling the FDA’s announcement of nusinersen’s approval ‘a Christmas surprise,’” Dr. Krainer commented. “For those of us who have had the thrilling experience of working on this drug from the very beginning, and have watched it succeed in reversing SMA pathology in animals—and more recently in young people with the illness—news of the approval is incredibly gratifying. Most gratifying to me is the thought that thousands of families will now be able to see their loved ones benefit from the drug’s therapeutic effects.”

“This drug will save lives of young people with severe SMA, and will improve the lives of many thousands of older children and adults who have disabling forms of the disease,” said Bruce Stillman, Ph.D., President and CEO of CSHL. “I join all of my colleagues at the Laboratory in congratulating Adrian Krainer for a magnificent achievement, made possible by decades of exquisitely performed fundamental research. This is a fantastic example of how basic research exploring the mechanisms of cells can lead to important clinical developments.”

Ionis Pharmaceuticals says nusinersen’s FDA approval under so-called Priority Review clears it for use in both pediatric and adult SMA patients. The drug, which is the first approved therapy for SMA, performed impressively in clinical trials testing its impact across a wide range of SMA patients, from just after birth to age 12 and beyond. The conclusion so far is that the earlier the drug is administered in patients, the more it helps them. A clinical study continues that is testing the drug’s ability to prevent the illness in newborns who are genetically destined to develop it.

All SMA patients share one aspect of pathology: they no longer have a working copy of a gene called SMN1 (“survival of motor neuron”). As its name implies, the gene encodes a protein essential for the development and survival of motor neurons. Without it, patients must rely on a nearly identical gene called SMN2. It’s a poor backup, though: the SMN2 gene (in all people) has a DNA error that usually prevents cells from manufacturing functioning SMN protein.

Dr. Krainer, a world authority on a cellular process called RNA splicing—the editing of RNA “messages” copied from our genes—conceived of a way to compensate for the error in SMN1 by correcting the defect in SMN2, which is caused by a failure of the splicing mechanism to “edit” the gene’s RNA message properly.

In coordination with Ionis scientists, Krainer’s team designed, synthesized and tested tiny molecules of modified RNA called antisense oligonucleotides (ASOs), which, when delivered to cells, bind at a specific site on the unedited RNA message made from the SMN2 gene. The ASO’s binding has the biochemical effect of fixing the splicing error responsible for non-functional SMN protein. In early tests, the ASO was delivered to the spinal cord of mice modeling SMA pathology. It was taken up by motor neurons and led them to manufacture functional SMN protein, which in turn had the effect of preventing SMA-like pathology. Human testing sponsored by Ionis began in 2011.

The data upon which the FDA’s approval of nusinersen was based included results from hundreds of patients. “Infantile-onset patients achieved and sustained clinically meaningful improvement in motor function compared to untreated study participants,” Ionis reported. In other, non-randomized, trials “some patients achieved milestones such as ability to sit unassisted, stand or walk when they would otherwise be unexpected to do so, and maintained milestones at ages when they would be expected to be lost,” Ionis said.

Emma LarsonEmma Larson, at a recent therapy session, continues to improve. Photo credit: Kathy Kmonicek (click to enlarge)One child who has benefited is Emma Larson, a lively 3½-year-old from Long Island, whose parents sought Dr. Krainer’s counsel when she was diagnosed with Type 2 SMA over two years ago. Dianne and Matthew Larson later enrolled Emma in a clinical trial, when she reached her 2nd birthday. She was already losing the ability to crawl, and to hold her head up without assistance. Within 2 months of receiving her first injections of nusinersen, Emma began to improve. “It was a miracle,” Dianne Larsen recalls. One day Emma crawled all the way from the living room to her mother’s bedroom, catching her completely by surprise. “I was freaking out! I couldn’t believe she had crawled all the way!” Dianne remembers. Today, Emma continues to receive injections and to improve. She is graduating from a walker to crutches, and getting ready to join her peers in preschool.

“We are in tears over here, along with the rest of the community! Amazing! Still numb,” Dianne said in an email the morning after the drug’s FDA approval. “Thank god for Adrian Krainer and all the people who made this drug possible!”

Dr. Stillman, echoing Dianne Larson’s joy, took the occasion to note that the applied research leading to nusinersen was preceded, in Krainer’s case, by some 15 years of basic research to determine the mechanisms that underlie RNA splicing. And those discoveries, Stillman noted, followed closely upon another great scientific triumph, occurring simultaneously at CSHL and MIT almost exactly 40 years ago.

“In the spring of 1977, Drs. Richard Roberts of CSHL and Phillip Sharp, then of MIT, first described RNA splicing—a fundamental mechanism in cells that regulates how our genes are expressed. Roberts and Sharp shared the 1993 Nobel Prize for that work, which then provided a point of departure for investigators like Adrian Krainer who worked on the mechanism. This is a perfect example of how basic research—with no specific purpose other than uncovering the mysteries of life—is the precondition for all the marvels of applied science that we enjoy, wonders that now include the development of nusinersen.”

About Cold Spring Harbor Laboratory

Founded in 1890, Cold Spring Harbor Laboratory has shaped contemporary biomedical research and education with programs in cancer, neuroscience, plant biology and quantitative biology. Home to eight Nobel Prize winners, the private, not-for-profit Laboratory employs 1,100 people including 600 scientists, students and technicians. The Meetings & Courses Program hosts more than 12,000 scientists from around the world each year on its campuses in Long Island and in Suzhou, China. The Laboratory's education arm also includes an academic publishing house, a graduate school and programs for middle and high school students and teachers. For more information, visit www.cshl.edu

Written by: Peter Tarr, Senior Science Writer | This email address is being protected from spambots. You need JavaScript enabled to view it. | 516-367-8455